Skip to content

Maxillary Sinus Augmentation Via the Bone Lid Technique

Maxillary Sinus Augmentation Via the Bone Lid Technique

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06222970
Acronym
SINUSLID_2023
Enrollment
40
Registered
2024-01-25
Start date
2020-05-04
Completion date
2024-12-31
Last updated
2024-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Maxillary Deficiency

Brief summary

Maxillary sinus augmentation is one of the most performed procedures to increase the bone quantity of the atrophic maxilla in order to allow implant placement. The aim of the present case series was to describe a surgical protocol to perform maxillary sinus augmentation with the bone lid technique, and its outcomes in a cohort of patients eligible for the procedure.

Interventions

PROCEDUREBone lid repositioning in course of sinus lift

A full-thickness flap was elevated to access the lateral maxillary bone wall. Subsequently, a lateral access window was prepared using a piezoelectric device with specific bone tips, delimitating a trapezoidal bone lid. Once the antrostomy was completed, the bone lid was gently removed with a Lucas surgical curette and anatomical tweezers, with great care to avoid damages to the Schneiderian membrane. The Schneiderian membrane was detached from the bone layer using specific sinus curettes. In case of sinus membrane perforation, the membrane was raised in all directions. All clinical cases received a cortical bone lamina to avoid graft particles displacement in the maxillary sinus. The elevated space was filled with chips of cortico-spongious bone. The antrostomy was then covered with the bone lid (osteotomy window), previously removed and preserved in physiological solution and fixed in the original anatomical position with a surgical glue. The flap was then repositioned and sutured.

Sponsors

University of Pisa
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Partially or fully edentulous patients requiring an implant-prosthetic rehabilitation of the premolar or molar maxillary areas with a residual ridge height lower than 4 mm. * Patients needing for a unilateral or bilateral sinus lift with a lateral wall approach.

Exclusion criteria

* Patients under treatment with immunosuppressive agents * Patients under treatment with medications that could impair bone metabolism. * Patients pregnant or breastfeeding. * Patients who had received irradiation treatment to the head and neck area. * Patients with uncontrolled diabetes. * Patients with uncontrolled periodontal disease.

Design outcomes

Primary

MeasureTime frameDescription
Bone gain6 monthsMeasurement of bone height and width

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026